The ferroportin disease

A new inherited disorder of iron metabolism, hereafter called “the ferroportin disease,” is increasingly recognized worldwide. The disorder is due to pathogenic mutations in the SLC40A1 gene encoding for a main iron export protein in mammals, ferroportin1/IREG1/MTP1, and it was originally identified...

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Veröffentlicht in:	Blood cells, molecules, & diseases molecules, & diseases, 2004-01, Vol.32 (1), p.131-138
1. Verfasser:	Pietrangelo, Antonello
Format:	Artikel
Sprache:	eng
Schlagworte:	Cation Transport Proteins - genetics Ferritins - blood Ferroportin Hemochromatosis Humans Iron Iron Metabolism Disorders - diagnosis Iron Metabolism Disorders - genetics Iron Metabolism Disorders - pathology Iron Overload - diagnosis Iron Overload - etiology Iron Overload - genetics Iron Overload - pathology Metal Metabolism, Inborn Errors - diagnosis Metal Metabolism, Inborn Errors - genetics Metal Metabolism, Inborn Errors - pathology
Online-Zugang:	Volltext
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